Are you an M.Pharm graduate looking to build a rewarding career in Drug Regulatory Affairs? Here’s an exciting opportunity for professionals with 1–5 years of experience who are passionate about regulatory submissions, dossier preparation, and global market approvals. 🌍✨
A reputed pharmaceutical organization, Sun Pharmaceutical Industries Ltd. is inviting applications for the position of Drug Regulatory Affairs Executive at its Vadodara location.
If you have experience handling regulatory documentation and lifecycle management for international markets—especially the MENA (Middle East & North Africa) region—this could be your next big career move! 📈
📍 Job Details at a Glance
- Position: Drug Regulatory Affairs Executive
- Location: Vadodara, Gujarat
- Experience Required: 1–5 years
- Qualification: M.Pharm
- Industry: Pharmaceutical / Regulatory Affairs
- Email to Apply: Rosemary.varghese@sunpharma.com
🧾 Key Responsibilities
This role focuses on ensuring smooth regulatory approvals and maintaining compliance standards for pharmaceutical products in MENA markets.
📑 1. Regulatory Submissions
- Preparation and submission of new product dossiers
- Filing variations and amendments as per regulatory guidelines
- Ensuring compliance with country-specific regulatory requirements
📊 2. Query Responses & Regulatory Coordination
- Preparing accurate and timely responses to authority queries
- Coordinating with QA, R&D, and Manufacturing teams
- Monitoring submission timelines and approval status
🔄 3. Life Cycle Management
- Managing post-approval changes
- Handling renewals and compliance documentation
- Maintaining updated regulatory databases
🌍 4. MENA Market Compliance
- Understanding Middle East & North Africa regulatory requirements
- Aligning CTD/eCTD dossiers as per regional guidelines
- Tracking regulatory updates and policy changes
🎯 Why Choose a Career in Drug Regulatory Affairs?
Regulatory Affairs is one of the fastest-growing domains in the pharmaceutical industry. With global expansion and stricter compliance standards, skilled regulatory professionals are in high demand.
✔ High global demand
✔ Opportunities in international markets
✔ Competitive salary growth
✔ Exposure to global regulatory systems
✔ Strategic role in product approvals
If you enjoy documentation, compliance processes, and cross-functional coordination, this field offers long-term stability and career progression. 📈💼
🧠 Skills Required
To succeed in this role, candidates should have:
- Strong knowledge of CTD / eCTD dossier preparation
- Understanding of regulatory guidelines for MENA markets
- Good communication and documentation skills
- Analytical thinking with attention to detail
- Strong time management and deadline adherence
Experience in lifecycle management and regulatory variations will be an added advantage. 👍
🎓 Who Can Apply?
Candidates meeting the following criteria are encouraged to apply:
- M.Pharm (Regulatory Affairs / Pharmaceutics preferred)
- 1–5 years of experience in regulatory submissions
- Knowledge of international regulatory frameworks
- Willingness to work from Vadodara
Freshers with strong regulatory internship exposure and documentation experience may also consider applying.
📈 Career Growth Opportunities
Working in Regulatory Affairs at Sun Pharmaceutical Industries Ltd. can open doors to:
- Senior Regulatory Executive roles
- Global Regulatory Strategy positions
- Regulatory Project Management
- International Regulatory Affairs roles
- Quality & Compliance Leadership
With experience, professionals can transition into regulatory markets such as US, EU, GCC, and ASEAN regions. 🌍
🏢 Why Vadodara?
Vadodara is emerging as a strong pharmaceutical and industrial hub in Gujarat. The city offers:
- Growing pharma & manufacturing ecosystem
- Good connectivity and infrastructure
- Affordable cost of living
- Better work-life balance
It’s an ideal destination for pharma professionals seeking stable long-term growth. 🏙️
📬 How to Apply?
Interested candidates can share their updated CV directly to:
📧 Rosemary.varghese@sunpharma.com
Suggested Email Subject Line:
Application for Drug Regulatory Affairs – Vadodara
Make sure your resume highlights:
- Regulatory submission experience
- Markets handled (especially MENA countries)
- Dossier preparation expertise
- Lifecycle management exposure
📝 Tips to Strengthen Your Application
✨ Highlight specific submissions handled
✨ Mention countries worked on in the MENA region
✨ Add measurable achievements (e.g., approvals secured)
✨ Keep your resume concise and compliance-focused
Recruiters in regulatory affairs prioritize clarity, compliance expertise, and documentation accuracy.
🌟 Final Thoughts
The pharmaceutical industry continues expanding globally, and regulatory professionals play a crucial role in ensuring product approvals and compliance across borders. If you are passionate about regulatory science, international documentation, and lifecycle management, this opportunity in Vadodara is worth exploring.
Take the next step in your regulatory career today! 🚀
